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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073094inversion1nstd229human GRCh38 chr22: 22,618,607-30,089,219 , GRCh37.p13 chr22: 22,961,077-30,485,208 BCRP1, POM121L10P, 237 more genes
    nsv7068065inversion1nstd229human GRCh38 chr22: 27,585,838-32,538,391 , GRCh37.p13 chr22: 27,981,799-32,934,377 LOC105372995, NEFH, 147 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7026825copy number variation1nstd229human GRCh38 chr22: 29,550,731-29,582,339 , GRCh37.p13 chr22: 29,946,720-29,978,328 NIPSNAP1, THOC5
    nsv7020483copy number variation1nstd229human GRCh38 chr22: 29,545,278-29,573,926 , GRCh37.p13 chr22: 29,941,267-29,969,915 NIPSNAP1, THOC5
    nsv6598656inversion1nstd223human GRCh38 chr22: 29,504,687-29,505,852 , GRCh37.p13 chr22: 29,900,676-29,901,841 THOC5
    nsv6598419inversion1nstd223human GRCh38 chr22: 29,513,207-29,514,267 , GRCh37.p13 chr22: 29,909,196-29,910,256 THOC5
    nsv6597486inversion1nstd223human GRCh38 chr22: 29,513,092-29,514,502 , GRCh37.p13 chr22: 29,909,081-29,910,491 THOC5
    nsv6596825inversion1nstd223human GRCh38 chr22: 29,515,007-29,515,678 , GRCh37.p13 chr22: 29,910,996-29,911,667 THOC5
    nsv6596349inversion1nstd223human GRCh38 chr22: 29,506,531-29,507,054 , GRCh37.p13 chr22: 29,902,520-29,903,043 THOC5
    nsv6548508copy number variation1nstd223human GRCh38 chr22: 29,540,110-29,551,172 , GRCh37.p13 chr22: 29,936,099-29,947,161 THOC5
    nsv6538774copy number variation1nstd223human GRCh38 chr22: 29,445,909-29,773,499 , GRCh37.p13 chr22: 29,841,898-30,169,488 ZMAT5, CABP7, 7 more genes
    nsv6311263copy number variation1nstd102humanUncertain significance GRCh37 chr22: 29,083,885-34,046,674 , GRCh38.p12 chr22: 28,687,897-33,650,688 SNORD125, LOC107985533, 145 more genes
    nsv6224574copy number variation1nstd214human GRCh38 chr22: 29,509,608-29,509,657 , GRCh37.p13 chr22: 29,905,597-29,905,646 THOC5
    nsv6222455copy number variation1nstd214human GRCh38 chr22: 29,552,634-29,552,710 , GRCh37.p13 chr22: 29,948,623-29,948,699 THOC5
    nsv6214329copy number variation1nstd214human GRCh38 chr22: 29,509,608-29,509,707 , GRCh37.p13 chr22: 29,905,597-29,905,696 THOC5
    nsv6134119copy number variation1nstd213human GRCh37 chr22: 29,540,000-30,070,001 , GRCh38.p12 chr22: 29,144,012-29,674,012 AP1B1, EWSR1, 19 more genes
    nsv6134118copy number variation1nstd213human GRCh37 chr22: 27,870,000-35,640,001 , GRCh38.p12 chr22: 27,474,039-35,244,008 AP1B1, EWSR1, 172 more genes
    nsv6106398insertion1nstd212human GRCh38 chr22: 29,553,905-29,553,905 , GRCh37.p13 chr22: 29,949,894-29,949,894 NIPSNAP1, THOC5
    nsv6056399copy number variation1nstd212human GRCh38 chr22: 29,509,659-29,509,757 , GRCh37.p13 chr22: 29,905,648-29,905,746 THOC5
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